Canonical Allele Identifier: CA804783358
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1298505030
gnomAD v3: 5-1415941-G-GC
gnomAD v4: 5-1415941-G-GC
MyVariant Identifiers: chr5:g.1416056_1416057insC (hg19) chr5:g.1415941_1415942insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1415943dup , CM000667.2:g.1415943dup GRCh38
NC_000005.9:g.1416058dup , CM000667.1:g.1416058dup GRCh37
NC_000005.8:g.1469058dup NCBI36
NG_015885.1:g.34487dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1031+156dup MANE Select ENSP00000270349.9:n.1031+156dup
ENST00000270349.11:c.1031+156dup ENSP00000270349.9:n.1031+156dup
ENST00000511750.1:n.481+156dup
NM_001044.4:c.1031+156dup NP_001035.1:n.1031+156dup
NM_001044.5:c.1031+156dup MANE Select NP_001035.1:n.1031+156dup
Search 100 bp 5'
Search 100 bp 3'